| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001003684.1 | 169 | Missense Mutation | ATC,GTC | I47V | NP_001003684.1 |
| NM_013387.3 | 169 | Missense Mutation | ATC,GTC | I47V | NP_037519.2 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001003692.1 | 169 | Intron | NP_001003692.1 | ||
| NM_001318129.1 | 169 | Intron | NP_001305058.1 | ||
| NM_019103.2 | 169 | Intron | NP_061976.1 |